Key result
In hemodialysis patients, plasma sCD40L levels >7.6 ng/mL were associated with an increased risk of cardiovascular morbidity and mortality (36% vs 29%; HR 1.61, 95% CI 1.03-3.11).
Why the study?
Does elevated soluble CD40 ligand predict combined cardiovascular morbidity and mortality in patients on haemodialysis?
Observational (n=300)
Yes
Does elevated soluble CD40 ligand predict combined cardiovascular morbidity and mortality in patients on haemodialysis?
Hazard Ratio: 1.61 (95% CI 1.03–3.11)
Absolute Event Rate: 36% vs 29%
p-value: p=<0.01
Elevated soluble CD40 ligand levels are an independent predictor of cardiovascular morbidity and mortality in hemodialysis patients.
May support risk stratification in hemodialysis; leaves open whether sCD40L modulation improves outcomes.
BACKGROUND: We tested the hypothesis that soluble CD40 ligand (sCD40L), a biomarker of proatherogenic inflammation, may be predictive of cardiovascular (CV) events in a subgroup of patients from the RISCAVID study, an observational and prospective study in patients on haemodialysis (HD). METHODS: Plasma sCD40L levels were assessed at the time of the enrollment in 300 HD patients (mean age: 65 ± 15 years), recruited in five different centres. During a follow-up of 24 months, overall mortality, CV mortality and CV major nonfatal events (acute myocardial infarction, congestive heart failure and stroke) were registered. Cox proportional hazards regression assessed adjusted differences in CV morbidity and mortality risk. RESULTS: Stratifying patients according to plasma sCD40L levels in those with levels lower or equal to (sCD40L-) and greater than (sCD40L+) the median value of 7.6 ng/mL, no significant difference was observed at baseline between the two groups in age, gender, blood pressure values and previous CV events. At 24-month follow-up, a significant (P < 0.01) lower incidence of the combined end point of CV morbidity and mortality was observed in the sCD40L- group (29%) as compared to the sCD40L+ group (36%). In the multivariate Cox proportional hazards regression model, the presence of sCD40L above the median value is associated with a significant increase in the risk of CV morbidity and mortality (hazard ratio: 1.61, 95% confidence interval 1.03-3.11). CONCLUSIONS: These observational results support the prognostic value of sCD40L in end-stage renal disease, thus providing a useful tool to better stratify CV prognosis in these patients.
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Desideri et al. (2011) conducted an observational in haemodialysis (n=300). Plasma sCD40L > 7.6 ng/mL vs. Plasma sCD40L ≤ 7.6 ng/mL was evaluated on combined end point of CV morbidity and mortality (HR 1.61, 95% CI 1.03-3.11, p=<0.01). In hemodialysis patients, plasma sCD40L levels >7.6 ng/mL were associated with an increased risk of cardiovascular morbidity and mortality (36% vs 29%; HR 1.61, 95% CI 1.03-3.11).
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